The Food and Drug Administration FDA Agency or we is proposing to revoke the regulations entitled Mutual Recognition of Pharmaceutical Good Manufacturing Practice Reports Medical Device Quality System Audit Reports and Certain Medical Device Product Evaluation Reports: United States and The European Community. FDA is proposing this action because the existing regulations have been superseded in part by the United States-European Union Amended Sectoral Annex for Pharmaceutical Good Manufacturing Practices GMPs that entered into force in 2017 2017 Amended Pharmaceutical Annex are outdated do not reflect current Agency practice and are unnecessary.